Accupril

Product NDC
0071-0527
11-digit product format
000710527
Labeler code
0071
Product ID
0071-0527_140c689b-e8c8-4db9-9bcf-c68869e0d762
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
quinapril hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Parke-Davis Div of Pfizer Inc
Application
NDA019885
Marketing category
NDA
Marketing start
1991-11-19
Marketing end
0000-00-00
Substance
QUINAPRIL HYDROCHLORIDE
Active strength
5 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0071-0527-23EA - Each0071-05273441dd47-4c4a-4c56-99b6-09a781e9c09712012-07-24
0071-0527-40EA - Each0071-0527633fb915-fd14-441a-9013-267cf805779712012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0071-0527ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED ACCUPRIL (QUINAPRIL) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]26Legacy NDC20250119_63cf5651-d52c-4d27-9fd4-ed9cd9724dff.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0071-0527-230007105272390 TABLET, FILM COATED in 1 BOTTLE (0071-0527-23) 1991-11-190000-00-00NoNoCurrent
0071-0527-4000071052740100 BLISTER PACK in 1 CARTON (0071-0527-40) > 1 TABLET, FILM COATED in 1 BLISTER PACK100 blister pack1991-11-190000-00-00NoNoCurrent